Dose-Response Impact of Glucosyl-Hesperidin (CitraPeak) on Exercise Performance, Blood Flow, Stress, Cognition, and Other Perceptual Indicators

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-50
SponsorLindenwood University

About this trial

The purpose of this study is to evaluate the dose-dependent effects of glucosyl-hesperidin (CITRAPEAK) supplementation on exercise performance, recovery indicators, blood flow, cognitive function, mood, sleep, and fuel utilization in recreationally active adults.

Eligibility criteria

Qualifiers

Participants who are between 18 - 50 years of age

Body mass index values will range from >25.0 < 30.0 kg/m2

The average body mass index for entire study cohort will be less than 27.0 kg/m2. As such an ongoing calculation of the recruited cohort's mean body mass index will be maintained and people will only be randomized into the study if the average cohort body mass index value does not exceed 27.0 kg/m2

Free-living and independent

Disqualifiers

Not currently completing at least 180 minutes of moderate to vigorous exercise per week for the past 6 months

Positive medical history and/or is currently being treated for some form of heart disease, cardiovascular disease

Currently being treated for kidney disease, renal failure, or has dialysis performed on regular intervals

Has liver disease or some form of clinically diagnosed hepatic impairment

Trial design

Treatments tested in this trial

  • 400 mg CITRAPEAK® (glucosyl-hesperidin) supplementation
  • Placebo
  • 200 mg CITRAPEAK® (glucosyl-hesperidin) supplementation

Treatment groups

60 Participants
are divided into 3 treatment groups

Sponsors and collaborators

Lindenwood University

Lead sponsor

Increnovo LLC

Collaborator